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Clonal Hematopoiesis: Crossroads of Aging, Cardiovascular Disease, and Cancer: JACC Review Topic of the Week
Peter Libby1, Robert Sidlow2, Amy E Lin1
1Division of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Insights
Clonal hematopoiesis of indeterminate potential (CHIP) is a new cardiovascular risk factor. CHIP doubles the risk of heart disease and stroke, necessitating new management strategies.
Area of Science:
- Hematology
- Cardiovascular Medicine
- Genetics
Background:
- Clonal hematopoiesis of indeterminate potential (CHIP) is an emerging cardiovascular risk factor.
- It originates from somatic mutations in hematopoietic stem cells, leading to mutant leukocyte clones.
- CHIP is associated with increased risks of coronary heart disease, ischemic stroke, and heart failure.
Purpose of the Study:
- To explain CHIP and its implications for cardiovascular risk.
- To address clinical challenges in screening, risk assessment, and management of CHIP.
- To provide recommendations for multidisciplinary care and identify knowledge gaps.
Main Methods:
- Literature review and synthesis of current evidence on CHIP.
- Exploration of clinical quandaries and expert opinions.
- Development of recommendations for managing cardiovascular risk in CHIP patients.
Main Results:
- CHIP presents a significant, independent cardiovascular risk.
- Individuals with CHIP have a doubled risk of major cardiovascular events.
- Current management strategies for CHIP-related cardiovascular risk are not well-established.
Conclusions:
- CHIP is a critical, non-traditional risk factor requiring attention from hematologists and cardiologists.
- Further research is needed to establish evidence-based screening and management guidelines.
- Multidisciplinary collaboration is essential for optimal patient care.
Abstract:
A novel, common, and potent cardiovascular risk factor has recently emerged: clonal hematopoiesis of indeterminate potential (CHIP). CHIP arises from somatic mutations in hematopoietic stem cells that yield clonal progeny of mutant leukocytes in blood. Individuals with CHIP have a doubled risk of coronary heart disease and ischemic stroke, and worsened heart failure outcomes independent of traditional cardiovascular risk factors. The recognition of CHIP as a nontraditional risk factor challenges specialists in hematology/oncology and cardiovascular medicine alike. Should we screen for CHIP? If so, in whom? How should we assess cardiovascular risk in people with CHIP? How should we manage the excess cardiovascular risk in the absence of an evidence base? This review explains CHIP, explores the clinical quandaries, strives to provide reasonable recommendations for the multidisciplinary management of cardiovascular risk in individuals with CHIP, and highlights current knowledge gaps.
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